10 reports of this reaction
1.9% of all EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL reports
#11 most reported adverse reaction
DEHYDRATION is the #11 most commonly reported adverse reaction for EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL, manufactured by Kenvue Brands LLC. There are 10 FDA adverse event reports linking EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL to DEHYDRATION. This represents approximately 1.9% of all 537 adverse event reports for this drug.
Patients taking EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL who experience dehydration should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DEHYDRATION is a less commonly reported adverse event for EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL, but still significant enough to appear in the safety profile.
In addition to dehydration, the following adverse reactions have been reported for EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL:
The following drugs have also been linked to dehydration in FDA adverse event reports:
DEHYDRATION has been reported as an adverse event in 10 FDA reports for EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEHYDRATION accounts for approximately 1.9% of all adverse event reports for EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL, making it a notable side effect.
If you experience dehydration while taking EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.